Trials / Terminated
TerminatedNCT04821973
Respiratory Tele Monitoring COVID 19 (TMR COVID-19)
Interest of Respiratory Tele Monitoring in COVID-19 Pneumonia
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Assistance Publique Hopitaux De Marseille · Academic / Other
- Sex
- All
- Age
- 10 Years
- Healthy volunteers
- Not accepted
Summary
The determinants of the evolution to a severe form for COVID-19 pneumonia remain unclear. COVID-19 pneumonia is characterized by a hypoxemia with a possible rapid worsening and related resuscitation requirement. The monitoring of patients in hospital wards (excluding intensive care unit) is therefore both necessary and complicated given the contagious risks for health workers. The COVID 19 Respiratory Tele Monitoring (RTM COVID 19) research project is based on a comparison between usual nurse respiratory monitoring (4 to 6 time per day) of respiratory parameters (capillary oxygen saturation, respiratory rate, hearth rate) and a continuous monitoring of these respiratory parameters with continuous monitoring by a portable, wireless and stand-alone device. The main objective of this work is a more sensitive and earlier detection of respiratory degradation events in patients with COVID-19 pneumonia (capillary desaturation, increased respiratory rate) requiring the introduction of oxygen therapy, its increase or a resuscitation requirement with possible intensive care admission. A prospective, randomized, multicentre, comparative exposure study will be conducted with planned inclusion of 80 patients. This investigation will focus on patients with COVID-19 pneumonia hospitalized in dedicated medical wards of two University Hospitals in France. A randomization will be stratified by Hospital and adapted so that each Hospital provides the same number of subjects in each arms: * Control Respiratory Monitoring Group (40 patients) * Experimental Respiratory Monitoring Group (40 patients) The main criterion is respiratory degradation event, during a 4 days period after ward admission, which motivates a change in the therapeutic strategy defined by the presence of at least one of these elements: * Capillary saturation \< 94% (regardless of oxygen intake) for at least 2 minutes. * And/or an increase in respiratory rate \> 20/minute for at least 2 minutes. The modification of the therapeutic strategy is defined by: * Introduction of oxygen therapy for included patients without oxygen therapy or supplementation of oxygen therapy \> 2 litres/minutes for included patients with oxygen therapy * And/or introduction of a high oxygen concentration mask * And/or Request an On-Site Opinion from a member of the resuscitation team. * And/or Transfer to intensive care or resuscitation unit * And/or Need for immediate resuscitation for life-threatening distress.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Radius PPG Tetherless Pulse Oximetry (Masimo) | continuous monitoring by a portable, wireless and stand-alone device |
| DEVICE | usual monitoring | usual nurse respiratory monitoring |
Timeline
- Start date
- 2020-09-22
- Primary completion
- 2021-05-26
- Completion
- 2021-05-26
- First posted
- 2021-03-30
- Last updated
- 2024-06-24
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04821973. Inclusion in this directory is not an endorsement.